Therapeutic Nanosystems for Oral Administration of Insulin

被引:0
作者
do Carmo, Flavia A. [1 ]
Sathler, Plinio C. [1 ]
Zancan, Patricia [1 ]
Rodrigues, Carlos R. [1 ]
Castro, Helena C. [2 ]
de Sousa, Valeria P. [1 ]
Sola-Penna, Mauro [1 ]
Cabral, Lucio M. [1 ]
机构
[1] Univ Fed Rio de Janeiro, CCS, Fac Pharm, BR-21941901 Rio De Janeiro, Brazil
[2] Univ Fed Fluminense, LABiEMol, Niteroi, RJ, Brazil
关键词
Bioavailability; diabetes mellitus; insulin; nanotechnology; oral administration; IN-VIVO; POLYMERIC HYDROGELS; LOADED LIPOSOMES; DELIVERY-SYSTEM; BILE-SALTS; NANOPARTICLES; ABSORPTION; MICROPARTICLES; DEGRADATION; STABILITY;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The treatment of Diabetes Mellitus (DM), a chronic disease, is primarily based upon administration of insulin forms to patients. Conventional subcutaneous administration is associated with a large number of complications, therefore, several new strategies have been developed. Amongst these strategies, oral insulin administration is much less invasive and, therefore, well tolerated. In recent years, various nanoformulations were developed for the oral administration of insulin, allowing more effective stabilization of the active pharmaceutical ingredient and modified for better absorption along the gastrointestinal tract. The development of different oral insulin nanoformulations in academic research as well as in patents, including the development of nanoparticles, liposomes, nanoemulsions and the use of cyclodextrins deserves special attention. The future of oral insulin nanoformulations is dependent on strategies utilizing simple technologies that stabilize the raw material, including inclusion within cyclodextrins or inclusion in low weight molecular mass polymers/oligomers. All of the theories developed here provide a solid foundation upon which to develop new methods for the production of pharmaceutical peptide formulations. In addition, the effective search for existing nanometric formulations of insulin could provide economically viable therapeutic options that can consequently be produced on an industrial scale.
引用
收藏
页码:620 / 628
页数:9
相关论文
共 68 条
[1]   Radiation synthesis of multifunctional polymeric hydrogels for oral delivery of insulin [J].
Abou Taleb, Manal F. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2013, 62 :341-347
[2]   Improved Stability and Antidiabetic Potential of Insulin Containing Folic Acid Functionalized Polymer Stabilized Multi layered Liposomes Following Oral Administration [J].
Agrawal, Ashish Kumar ;
Harde, Harshad ;
Thanki, Kaushik ;
Jain, Sanyog .
BIOMACROMOLECULES, 2014, 15 (01) :350-360
[3]  
[Anonymous], 2011, DIABETES MANAGE, DOI DOI 10.2217/DMT.10.5
[4]   Novel thermo- and pH-responsive hydroxypropyl cellulose- and poly (L-glutamic acid)-based microgels for oral insulin controlled release [J].
Bai, Yunyan ;
Zhang, Zhe ;
Zhang, Aiping ;
Chen, Li ;
He, Chaoliang ;
Zhuang, Xiuli ;
Chen, Xuesi .
CARBOHYDRATE POLYMERS, 2012, 89 (04) :1207-1214
[5]  
Bhadoria M.S., 2013, INT J RES COMPUT ENG, P2
[6]  
Black C, 2007, Health Technol Assess, V11, P1
[7]   CHEMICAL-STABILITY OF INSULIN .1. HYDROLYTIC DEGRADATION DURING STORAGE OF PHARMACEUTICAL PREPARATIONS [J].
BRANGE, J ;
LANGKJAER, L ;
HAVELUND, S ;
VOLUND, A .
PHARMACEUTICAL RESEARCH, 1992, 9 (06) :715-726
[8]   A review of the efficacy and safety of nanoparticle-based oral insulin delivery systems [J].
Card, Jeffrey W. ;
Magnuson, Bernadene A. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2011, 301 (06) :G956-G967
[9]   Particle shape: A new design parameter for micro- and nanoscale drug delivery carriers [J].
Champion, Julie A. ;
Katare, Yogesh K. ;
Mitragotri, Samir .
JOURNAL OF CONTROLLED RELEASE, 2007, 121 (1-2) :3-9
[10]   Polymeric hydrogels for oral insulin delivery [J].
Chaturvedi, Kiran ;
Ganguly, Kuntal ;
Nadagouda, Mallikarjuna N. ;
Aminabhavi, Tejraj M. .
JOURNAL OF CONTROLLED RELEASE, 2013, 165 (02) :129-138